Activation and regulation of Toll-like receptors 2 and 1 in human leprosy

被引:245
作者
Krutzik, SR
Ochoa, MT
Sieling, PA
Uematsu, S
Ng, YW
Legaspi, A
Liu, PT
Cole, ST
Godowski, PJ
Maeda, YM
Sarno, EN
Norgard, MV
Brennan, PJ
Akira, S
Rea, TH
Modlin, RL [1 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Div Dermatol, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Microbiol & Immunol, Los Angeles, CA USA
[3] Osaka Univ, Japan Sci & Technol Corp, Microbial Dis Res Inst, Dept Host Def, Osaka, Japan
[4] Inst Pasteur, Unite Genet Mol Bacterienne, Paris, France
[5] Genentech Inc, Dept Mol Biol, San Francisco, CA 94080 USA
[6] Natl Inst Infect Dis, Leprosy Res Ctr, Dept Microbiol, Tokyo, Japan
[7] Inst Oswaldo Cruz, Leprosy Lab, BR-20001 Rio De Janeiro, Brazil
[8] Univ Texas, SW Med Ctr, Dept Microbiol, Dallas, TX USA
[9] Colorado State Univ, Dept Microbiol, Ft Collins, CO 80523 USA
[10] Univ So Calif, Sch Med, Dermatol Sect, Los Angeles, CA 90033 USA
关键词
D O I
10.1038/nm864
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The expression and activation of Toll-like receptors (TLRs) was investigated in leprosy, a spectral disease in which clinical manifestations correlate with the type of immune response mounted toward Mycobacterium leprae. TLR2-TLR1 heterodimers mediated cell activation by killed M. leprae, indicating the presence of triacylated lipoproteins. A genome-wide scan of M. leprae detected 31 putative lipoproteins. Synthetic lipopeptides representing the 19-kD and 33-kD lipoproteins activated both monocytes and dendritic cells. Activation was enhanced by type-1 cytokines and inhibited by type-2 cytokines. In addition, interferon (IFN)-gamma and granulocyte-macrophage colony-stimulating factor (GM-CSF) enhanced TLR1 expression in monocytes and dendritic cells, respectively, whereas IL-4 downregulated TLR2 expression. TLR2 and TLR1 were more strongly expressed in lesions from the localized tuberculoid form (T-lep) as compared with the disseminated lepromatous form (L-lep) of the disease. These data provide evidence that regulated expression and activation of TLRs at the site of disease contribute to the host defense against microbial pathogens.
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收藏
页码:525 / 532
页数:8
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